Research of Coffin-lowry Syndrome has been linked to Dwarfism, Severe Mental Retardation, Congenital Hand Deformities, Bone Diseases, Developmental, Cataplexy. The study of Coffin-lowry Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Coffin-lowry Syndrome include Translation, Localization, Startle Response, Osteoblast Differentiation, Exocytosis. These pathways complement our catalog of research reagents for the study of Coffin-lowry Syndrome including antibodies and ELISA kits against MAPK, S6 KINASE 2, RAS, ACTIVATING TRANSCRIPTION FACTOR 4, DMD.
Coffin-lowry Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Coffin-lowry Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 585 products for the study of Coffin-lowry Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Coffin-lowry Syndrome is also known as coffin-lowry syndrome, mental retardation with osteocartilaginous abnormalities, coffin-lowry syndrome (disorder), coffin lowry syndrome, mental retardation, coffin syndrome.